Shanghai Korain Biotech Co., Ltd

Shanghai Korain Biotech Co Ltd

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IGF1 Rat ELISA Kit , 1.55ng/ml Sensitivity Enzyme Linked Immunosorbent Assay Kit

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Shanghai Korain Biotech Co., Ltd
City:shanghai
Province/State:shanghai
Country/Region:china
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IGF1 Rat ELISA Kit , 1.55ng/ml Sensitivity Enzyme Linked Immunosorbent Assay Kit

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Brand Name :BT Lab
Model Number :Cat.No E0709Ra
Certification :CE, ISO9001:2005, MSDS
Place of Origin :Shanghai, China
MOQ :Negotiation
Price :Negotiation
Supply Ability :Western Union, T/T
Delivery Time :1-3 business days, bulk order within one week
Packaging Details :Wrapped with ice pack and styrofoam package
Target Protein :Insulin-like growth factor 1
Uniprot No. :P41159
Bulk Order :Yes
Assay Time :2 hours
Standard Curve Range :3ng/ml - 900ng/ml
Sensitivity :1.55ng/ml
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96 wells Rat High sensitivity IGF1 ELISA Kit

Cat.No E0709Ra

Standard Curve Range: 3ng/ml - 900ng/ml

Sensitivity: 1.55ng/ml

Size: 96 wells

Storage: Store the reagents at 2-8°C. For over 6-month storage refer to the expiration date keep it at -20°C. Avoid repeated thaw cycles. If individual reagents are opened it is recommended that the kit be used within 1 month.

* This product is for research use only, not for use in diagnosis procedures. It’s highly recommend to read this instruction entirely before use.

Reagent Provided

Components Quantity
Standard Solution (960ng/ml) 0.5ml x1
Pre-coated ELISA Plate 12 * 8 well strips x1
Standard Diluent 3ml x1
Streptavidin-HRP 6ml x1
Stop Solution 6ml x1
Substrate Solution A 6ml x1
Substrate Solution B 6ml x1
Wash Buffer Concentrate (30x) 20ml x1
Biotinylated Rat IGF-1 Antibody 1ml x1
User Instruction 1
Plate Sealer 2 pics
Zipper bag 1 pic

Material Required But Not Supplied

  • 37°C±0.5°C incubator
  • Absorbent paper
  • Precision pipettes and disposable pipette tips
  • Clean tubes
  • Deionized or distilled water
  • Microplate reader with 450 ± 10nm wavelength filter

Specimen Collection

Serum Allow serum to clot for 10-20 minutes at room temperature. Centrifuge at 2000-3000 RPM for 20 minutes.

Plasma Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 15 minutes at 2000-3000 RPM at 2 - 8°C within 30 minutes of collection.

Urine Collect by sterile tube. Centrifuge at 2000-3000 RPM for approximately 20 minutes. When collecting pleuroperitoneal fluid and cerebrospinal fluid, please follow the procedures above-mentioned.

Cell Culture Supernatant Collect by sterile tubes when examining secrete components. Centrifuge at 2000-3000 RPM for approximately 20 minutes. Collect the supernatants carefully. When examining the components within the cell, use PBS (pH 7.2-7.4) to dilute cell suspension to the cell concentration of approximately 1 million/ml. Damage cells through repeated freeze-thaw cycles to let out the inside components. Centrifuge at 2000-3000 RPM for approximately 20 minutes.

Tissue Rinse tissues in PBS (pH 7.4) to remove excess blood thoroughly and weigh before homogenization. Mince tissues and homogenize them in PBS (pH7.4) with a glass homogenizer on ice. Thaw at 2-8°C or freeze at -20°C. Centrifuge at 2000-3000 RPM for approximately 20 minutes.

Note

  • Sample concentrations should be predicted before being used in the assay. If the sample concentration is not within the range of the standard curve, users must contact us to determine the optimal sample for their particular experiments.

  • Samples to be used within 5 days should be stored at 2-8°C. Samples should be aliquoted or must be stored at -20°C within 1 month or -80°C within 6 months. Avoid repeated freeze thaw cycles.

  • Samples should be brought to room temperature before starting the assay.

  • Centrifuge to collect sample before use.

  • Samples containing NaN3 can’t be tested as it inhibits the activity of Horse Radish Peroxidase (HRP).

  • Collect the supernatants carefully. When sediments occurred during storage, centrifugation should be performed again.

* Sample can't be diluted with this kit. Owing to the the material we use to prepare the kit, the sample matrix interference may falsely depress the specificity and accuracy of the assay.

Calculation of Result

Construct a standard curve by plotting the average OD for each standard on the vertical (Y) axis against the concentration on the horizontal (X) axis and draw a best fit curve through the points on the graph. These calculations can be best performed with computer-based curve-fitting software and the best fit line can be determined by regression analysis.

References

Pellizas C.G., del Mar Montesinos M., Masini-Repiso A.M., Torres A.I., Coleoni A.H.
Thyroid 12:1071-1078(2002)

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